Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs387906458
rs387906458
F8
1 1.000 0.080 X 154904488 frameshift variant -/A delins 0.700 0
dbSNP: rs387906445
rs387906445
F8
1 1.000 0.080 X 154957112 frameshift variant -/C delins 0.700 0
dbSNP: rs387906459
rs387906459
F8
1 1.000 0.080 X 154904391 frameshift variant -/T delins 0.700 0
dbSNP: rs886039906
rs886039906
F8
3 1.000 0.080 X 154929022 frameshift variant -/TTGGTTAT ins 3.3E-05 0.700 0
dbSNP: rs387906437
rs387906437
F8
1 1.000 0.080 X 154969491 frameshift variant A/- del 0.700 0
dbSNP: rs137852458
rs137852458
F8
1 1.000 0.080 X 154896146 missense variant A/C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852475
rs137852475
F8
1 1.000 0.080 X 154992945 missense variant A/C snv 0.800 1.000 22 1989 2013
dbSNP: rs1466581271
rs1466581271
F8
1 1.000 0.080 X 154906448 missense variant A/C snv 0.700 1.000 20 1989 2002
dbSNP: rs137852377
rs137852377
F8
1 1.000 0.080 X 155022476 missense variant A/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852386
rs137852386
F8
1 1.000 0.080 X 154997011 missense variant A/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852400
rs137852400
F8
1 1.000 0.080 X 154969486 missense variant A/C snv 0.800 1.000 2 2011 2013
dbSNP: rs28937287
rs28937287
F8
1 1.000 0.080 X 154906470 missense variant A/C snv 0.800 1.000 2 2011 2013
dbSNP: rs2069762
rs2069762
IL2
23 0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 0.010 < 0.001 1 2018 2018
dbSNP: rs1405473814
rs1405473814
F8
1 1.000 0.080 X 154863109 missense variant A/C snv 0.700 0
dbSNP: rs28933670
rs28933670
F8
1 1.000 0.080 X 154966483 missense variant A/C;G snv 0.800 1.000 22 1989 2013
dbSNP: rs944567323
rs944567323
F8
1 1.000 0.080 X 154999538 missense variant A/C;G snv 0.700 0
dbSNP: rs137852383
rs137852383
F8
1 1.000 0.080 X 154997050 missense variant A/C;T snv 0.800 1.000 2 2011 2013
dbSNP: rs137852405
rs137852405
F8
2 0.925 0.080 X 154969405 missense variant A/G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852413
rs137852413
F8
1 1.000 0.080 X 154961131 missense variant A/G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852430
rs137852430
F8
1 1.000 0.080 X 154947853 missense variant A/G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852434
rs137852434
F8
1 1.000 0.080 X 154947782 missense variant A/G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852455
rs137852455
F8
1 1.000 0.080 X 154899946 missense variant A/G snv 0.800 1.000 22 1989 2013
dbSNP: rs28933669
rs28933669
F8
1 1.000 0.080 X 154966523 missense variant A/G snv 0.800 1.000 22 1989 2013
dbSNP: rs1189348665
rs1189348665
F8
1 1.000 0.080 X 154966663 missense variant A/G snv 0.700 1.000 20 1989 2002
dbSNP: rs1281943689
rs1281943689
F8
1 1.000 0.080 X 154993074 missense variant A/G snv 0.700 1.000 20 1989 2002